<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhan S</submitter><funding>Nanjing Drum Tower Hospital Clinical Research Special Fund Projec</funding><funding>National Natural Science Foundation of China</funding><funding>Nanjing Drum Tower Hospital Clinical Research Special Fund Project</funding><pagination>211</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12613488</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by dysregulated inflammatory response lacking reliable diagnosis biomarkers and therapy targets. Extracellular vesicles (EVs)-derived cargo as biomarkers and mediators of SLE have garnered significant attention, however, quantitative inflammatory protein profile of SLE EVs remain uncovered.&lt;h4>Objective&lt;/h4>Current study focuses on exploring the inflammatory protein landscape of SLE serum EVs via quantitative proximity extension assay (PEA) and evaluates their diagnostic utility for SLE and lupus nephritis (LN).&lt;h4>Methods&lt;/h4>In this cross-sectional study, we first utilized PEA to profile inflammatory proteins derived from serum EVs in 101 individuals, including 70 SLE patients and 33 healt</pubmed_abstract><journal>Arthritis research &amp; therapy</journal><pubmed_title>Inflammation-related proteomics of extracellular vesicles as novel biomarkers for systemic lupus erythematosus revealed by proximity extension assay.</pubmed_title><pmcid>PMC12613488</pmcid><funding_grant_id>2023-JCYJ-QP-25</funding_grant_id><funding_grant_id>2024-LCYJ-MS-11</funding_grant_id><funding_grant_id>82202600</funding_grant_id><pubmed_authors>Dou H</pubmed_authors><pubmed_authors>Zhan S</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Zhou S</pubmed_authors><pubmed_authors>Yang P</pubmed_authors><pubmed_authors>Ge M</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Shen H</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inflammation-related proteomics of extracellular vesicles as novel biomarkers for systemic lupus erythematosus revealed by proximity extension assay.</name><description>&lt;h4>Background&lt;/h4>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by dysregulated inflammatory response lacking reliable diagnosis biomarkers and therapy targets. Extracellular vesicles (EVs)-derived cargo as biomarkers and mediators of SLE have garnered significant attention, however, quantitative inflammatory protein profile of SLE EVs remain uncovered.&lt;h4>Objective&lt;/h4>Current study focuses on exploring the inflammatory protein landscape of SLE serum EVs via quantitative proximity extension assay (PEA) and evaluates their diagnostic utility for SLE and lupus nephritis (LN).&lt;h4>Methods&lt;/h4>In this cross-sectional study, we first utilized PEA to profile inflammatory proteins derived from serum EVs in 101 individuals, including 70 SLE patients and 33 healt</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T12:31:00.193Z</modification><creation>2026-05-16T03:12:50.509Z</creation></dates><accession>S-EPMC12613488</accession><cross_references><pubmed>41233846</pubmed><doi>10.1186/s13075-025-03681-x</doi></cross_references></HashMap>